* Plenary Speaker
Larry Anderson1, Dennis McGillicuddy1, Scott Doney1, Mat Maltrud2 and Frank Bryan3
The Role of Mesoscale Eddies in Basin-scale Biogeochemical Budgets of the North Atlantic
1 Woods Hole Oceanographic Institution, Woods Hole, MA 02543
2 Los Alamos National Laboratory, Los Alamos, NM 87545
3 National Center for Atmospheric Research, Boulder, CO 80307
ABSTRACT:
Four 4-year eddy-resolving (0.1-degree) simulations of nitrate
transport in the euphotic zone of the North and Equatorial Atlantic
have been conducted and are compared with data, coarse-resolution
simulations and previous modeling studies. Through the lifting of
nitrate-rich isopycnals into the euphotic zone, vertical advection by
mesoscale eddies dominates the transport of nitrate into the euphotic
zone of the permanently-stratified subtropical gyre.
Coarse-resolution simulations run with the Gent and McWilliams (1990)
mesoscale isopycnal mixing parameterization do not capture this
effectively diapycnal flux.
The seasonal cycle of the Antarctic Circumpolar Current at 170°W - Ecosystem structure, nutrient utilization and export flux.
1 Lamont-Doherty Earth Observatory, Palisades, NY 10964
ABSTRACT:
Among the three principal High-Nutrient Low-Chlorophyll regions
(Subarctic Pacific, Equatorial Pacific and Southern Ocean), the Southern
Ocean contains by far the largest inventory of surface nutrients. The
biological pump, measured in terms of the fraction of upwelled nutrients
converted to organic matter and exported to the deep sea, is clearly not
high in the Southern Ocean. Nutrient utilization efficiency in the
Southern Ocean is potentially an important factor within the array of
mechanisms by which ocean processes regulate the CO2 content of the
atmosphere. Consequently, much attention has been paid to this topic, and
many investigators have speculated about the relative importance of the
factors (light, grazing, iron) that potentially limit the growth of
phytoplankton and the consumption of nutrients in the Southern Ocean.
Studies conducted by US JGOFS in the SW Pacific sector of the
Southern Ocean provide an unprecedented view of the seasonal evolution of
the structure of the planktonic ecosystem, as well as of factors regulating
nutrient utilization and export of biogenic material to depth. Nutrient
utilization and export flux is intimately linked to the growth of large
diatom species, although diatoms are not the sole agent of export. At
various places, and at different times, light, grazing, iron and dissolved
silicic acid each play a limiting role. These complex relationships must
all be considered when simulating the sensitivity of the Southern Ocean's
biological pump to climate change.
Rob Armstrong1 and Mike Landry2
A model structure for analysis of food web data and for carbon cycle simulation
1 Marine Science Res. Center, Stony Brook Univ., Stony Brook, NY
2 Dept of Oceanography, Univ. of Hawaii, Honolulu, HI
ABSTRACT:
Previous size-structured models of marine food webs have proved
inadequate for analyzing food web data. In particular, the use of
discrete, non-overlapping "boxes" for size classes does not capture the
size plasticity of individual organisms, nor does it reflect the fact
that characteristic size differences among competing species may not be
the same as characteristic size differences between adjacent trophic
levels. Here we present a new food web model, with a parameterized
zooplankton size spectrum, that we believe will enable maximal information
to be extracted from food web data. This model structure should also be
useful in simulating ecosystem processes in food web models. Development
of this model was part of our ongoing collaborative project to model food
web transfers and export fluxes in pelagic ecosystems.
Reference:
Armstrong, R.A. Beyond Moloney and Field: A hybrid spectral model of plankton interaction. DSR II (submitted)
J.E. Bauer1, M.D. DeGrandpre2, P. Vlahos3, C.S. Hopkinson4, R.F. Chen5 and L.I. Aluwihare6.
Whole-Shelf and Slope Studies of Carbon Inventories and Fluxes in the Northwest Atlantic Continental Margin During the Ocean Margins Program
1 School of Marine Science/VIMS, College of Wm. & Mary, Gloucester Pt., VA 23062
2 University of Montana, Dept. of Chemistry, 32 Campus Dr., Missoula, MT 59812
3 University of Connecticut, Dept. of Marine Sciences,1084 Shennecossett Rd., Groton, CT 06340
4 Ecosystems Center, Marine Biological Laboratory, Woods Hole, MA 02543
5 University of Massachusetts, Dept. of Environmental, Coastal and Ocean Sciences, 100 Morrissey Blvd., Boston, MA 02125
6 Scripps Institute of Oceanography, Geosciences Research Division, 9500 Gilman Dr., La Jolla, CA 92093
ABSTRACT:
The DOE- and NSF-funded Ocean Margins Program undertook a comprehensive
evaluation of the inventories (including sources and inputs) and fluxes
of organic and inorganic carbon in shelf and slope waters of the Middle
Atlantic Bight (MAB) in the NW Atlantic from 1994-1996. These studies
included both whole-system shipboard surveys from Cape Cod to Cape Hatteras,
as well as autonomous measurements from moored arrays in the southern
portion of the study area. In spite of a long history of carbon-based
studies in this region, there have been no previously reported measurements
of either the partial pressure of
CO2
(pCO2)
or of dissolved organic carbon (DOC) for the MAB prior to 1994, thus
precluding the synthesis of a comprehensive carbon budget there.
Calculations based on air-sea
pCO2
differences indicate that the MAB is a net annual sink for atmospheric
CO2
with the inner, mid, and outer-shelf regions taking up ~0.1, 0.7, and 0.2
Mt C yr-1,
respectively, for a net uptake of
~1&plusnm;0.6 Mt C yr-1,
which is relatively small compared to the net influxes observed recently
in some other ocean margins. The annual cycle
of heating and cooling combined with high winds during the period of
undersaturation (winter) appears to account for a significant portion of
the uptake. The flux uncertainty is dominated by uncertainty of the gas
transfer velocity parameterization, atmospheric
CO2
levels, and coarse spatial
pCO2
resolution.
Concentrations of DOC were greater inshore than offshore and increased
southward along the shelf. The total DOC inventory on the shelf during
spring 1996 was estimated at
~5.88 x 1012 g C
and this increased by
0.4 x 1012 g C (7%)
by late summer. A simple mass balance of DOC input and export in the
MAB resulted in total export of
18.7 to 19.6 x 1012 g C y-1.
Although water budgets for the MAB suggest a
relatively small (~5-10%) input flux of DOC from land, a dual isotopic
(14C and
13C)
approach and multi-source model suggests that as much
as half of the total bulk DOC, and even greater fraction of the
suspended POC, originates from terrigenous sources that have become
highly aged either on land or in the MAB. On average, the C:N:P
ratio of shelf DOM (431:36:1) was substantially higher than Redfield,
but not nearly as high as that of deep slope water (2700:215:1); the
selective bacterial remineralization of P and N from DOM was further
confirmed by incubation studies. The presence of a young, bomb
14C-enriched
polysaccharide fraction was observed in the
>1kDalton DOM fraction, and may be representative of the more labile
and semi-labile components of DOM in this system.
D. Bogucki1 and L. G. Redekopp2
Absolute and convective instabilities in air-water interface
1 RSMAS
2 USC
ABSTRACT:
Current estimates of air-sea gas exchange vary by over a factor of two
depending on the parameterization of the transfer velocity from
wind speed. Uncertainties in the parameterization occur because wind
speed is indicative of, but not necessarily an accurate descriptor for,
the local characteristics of the air-water interface in the presence
of both the air and water boundary layers.
To obtain greater insight to the dynamics of the air-water boundary
layer, we are investigating a generalized Holmboe model of the
air-water interface.
We analytically investigate the onset of instabilities considering both
spatial and temporal modes, with the goal of identifying conditions for
spontaneous onset of intrinsic dynamics that are not dependent on the
spatial history of the flow. The results will be compared to
observations from tank experiments in the future.
Magnitude, Variability and Controls on the Ratio of Particle Export to Primary Production in the Upper Ocean
1 Woods Hole Oceanographic Institution Woods Hole, MA 02543 USA tel: 508-289-2309; fax: 508-457-2193 email: kbuesseler@whoi.edu
ABSTRACT:
The transport of biogenic particles from the surface to the deep ocean is
the key driver of the ocean's biological pump. Globally, the magnitude and
efficiency of the biological pump will in part modulate levels of atmospheric
CO2, and from the geological paleo-oceanographic record there is evidence
of elevated rates of export of POC resulting from changes in the functioning
of the pump. Thus there is a need to better understand what are the key
determinants of this pump in the present day, and how they might be altered
in response to climate change. This SMP project and poster examine the
present day relationship between primary production and particulate export
in the upper ocean. Recent advances in satellite derived algorithms for
primary production lend well to improved global predictions of the rate of
C uptake, however our ability to determine particle fluxes is much poorer.
A pronounced mismatch between spatial patterns in primary production and
the export of carbon to the deep ocean, points to the complex suite of
transformations that occur in the upper 300 m of the ocean. The results
thus far indicate that the relative rates of C uptake and losses via
sinking particles vary as a function of the local food web dynamics. In
particular, diatoms appear to play an important role in enhancing the ratio
of export:production in the upper ocean. In spite of the recent development
of promising modeling approaches to assess export production on global
scales (Laws et al., 2000), our understanding of the key processes
determining what controls the efficiency of particle transport between the
surface and deep ocean remains weak. Results from a recent synthesis of the
AESOPS data along the Polar Front will be highlighted in this poster,
as well as an update on the compilation of a global shallow POC flux budget
as part of this SMP project.
Mary-Elena Carr1, Marjorie Friedrichs2 and Ahmed H. Ali1
Marine primary production estimates from ocean color: a comparative study of algorithms
1 Jet Propulsion Laboratory, California Institute of Technology
2 Old Dominion Unversity
ABSTRACT:
The Primary Production Algorithm Round Robin 3 (PPARR3) aims to compare
models or algorithms that estimate marine primary production from
satellite measurements of ocean color (PP models). It is a continuation
of previous PPARR exercises, which compared in situ carbon14
uptake rates with an estimate of primary production using
satellite-accessible data. PPARR2 found that modeled primary production
would be within a factor of two of the in situ rates if systematic
offsets were corrected. PPARR3 aims to provide a forum to compare model
output, improve parameterization, and help identify the source of
biases. This community project presently counts with over twenty
modeling groups who estimate primary production for input fields
provided by the organizers. The PPARR3 exercise consists of 3 stages, the
first stage is a comparison of monthly global primary production fields
generated by the different algorithms. Stage 2 is a step-by-step
sensitivity study of the different algorithms tracking the derivation
of sub-products in a series of point value estimates. The third stage
is similar to PPARR1 and PPARR2 and is a blind comparison to the
quality-controlled data base of carbon-14 measurements in the
equatorial Pacific. We present here the results of the first stage, which
compares the output of the models throughout an annual cycle.
Takamitsu Ito1, Mick Follows1,and John Marshall1
An idealized model of tracer transport and ventilation in the Southern Ocean.
1 Program in Atmospheres Oceans and Climate, Dept Earth, Atmospheric and Planetary Sciences, Massachusetts Inst. of Technology, Cambridge, MA 02139
ABSTRACT:
We construct a zonally-averaged model of tracer transport and air-sea
gas exchanges in the Southern Ocean based on the residual mean theory.
Given the surface wind stress and the surface buoyancy forcing,
the idealized theory can predict the interior stratification and
the meridional overturning circulation (MOC) in the vicinity of
the Antarctic Circumpolar Current (ACC).
We evaluate the simple theory by calculating the time-varying,
zonally-averaged distribution of CFCs in the region of the ACC and
comparing to observations from the WOCE survey. We find that
the simple theory captures the broad structure of ventilation of
CFCs into the thermocline and intermediate waters very well, and
can be extended to represent the formation of deep waters,
produced by the insense buoyancy fluxes near Antarctica. The
simplicity of the model allows a clear examination of the
relationships between the physical forcing, eddy transfer mechanisms
and tracer transports.
We discuss the sensitivities of the ventilation of CFCs to the imposed
surface wind stress and the buoyancy forcing. We find that the
ventilation of CFCs into the thermocline and intermediate waters is
controlled both by advection in the residual circulation and isopycnal
eddy stirring. The vigor of the residual circulation and MOC is most
sensitive to the amplitiude and patterns of surface buoyancy fluxes
while the isopycnal stirring of tracers is sensitive to the surface wind
stress. This idealized model provides insights into the mechanisms
controlling the ventilation of tracers into the oceans and in
more complex, three-dimensional general circulation models and can
be extended to consider biogeochemically active tracers.
F. Chai1, M.-S. Jiang1, R. T. Barber2, R. C. Dugdale3 and Y. Chao4
Interdecadal Variation of the Transition Zone Chlorophyll Front, A Physical-Biological Model Simulation between 1960 and 1990
1 School of Marine Sciences, University of Maine, Orono, ME 04469-5741
2 Duke University, NSOE Marine Laboratory, 135 Duke Marine Lab Road, Beaufort, NC 28516
3 Romberg Tiburon Center, San Francisco State University, PO Box 855, Tiburon CA 94920
4 Jet Propulsion Laboratory, 4800 Oak Grove Drive, Pasadena, CA 91109
ABSTRACT:
The Transition Zone Chlorophyll Front (TZCF) separates the low chlorophyll
subtropical gyres and the high chlorophyll subarctic gyres in the Pacific
Ocean. The interdecadal climate variability affects marine ecosystems in
both subtropical and subarctic gyres, consequently the position of the TZCF.
A three-dimensional physical-biological model has been used to study
interdecadal variation of the TZCF using a retrospective analysis of a
30-year (1960-1990) model simulation. The physical-biological model is
forced with the monthly mean heat flux and surface wind stress from the
Comprehensive Ocean Atmosphere Data Set.
The modeled position of the TZCF, operationally defined as the isopleth of
0.2 mg/m3 chlorophyll, is located between 25°N and 27°N in the
central North
Pacific during the winter and between 33°N and 35°N during the summer, which
agrees with the seasonal migration patterns of the TZCF detected with
SeaWiFS. The modeled winter MLD shows the largest increase between 30°N and
40°N in the central North Pacific (150°E to 180°), with a value of 40-60%
higher (deeper mixed layer) during 1979-90 relative to 1964-75 values. In
the subarctic gyre in both northeast (Ocean Station Papa, OSP) and northwest
Pacific (Oyashio region), the modeled winter MLD decreases by about 20%
during the period of 1979-90 relative to 1964-75 levels. The winter Ekman
pumping velocity difference between 1979-90 and 1964-75 shows the largest
increase is located between 30°N and 45°N in the central and eastern North
Pacific (180 to 150°W). In the subarctic northeast Pacific region including
the Gulf of Alaska, the winter Ekman pumping velocity decreases during the
period of 1979-90, but its value increases in the northwest Pacific
(Oyashio region) after 1976-77 climatic shift. The modeled winter surface
nitrate difference between 1979-90 and 1964-75 shows increase in the
latitudinal band of 30°N and 45°N from the west to the east (135°E-135°W),
the modeled nitrate concentration is about 10 to 50% higher in general
during the period of 1979-90 relative to 1964-75 values depending upon
location. The increase of the winter surface nitrate concentration during
1979-90 is caused by a combination of the winter MLD increase and the
winter Ekman pumping enhancement after 1976-77 climatic shift. The modeled
nitrate concentration increase after 1976-77 lead to the primary
productivity increase in the central North Pacific (30°N-40°N and
180°-140°W). Enhanced primary productivity after the 1976-77 climatic
shift contributes higher phytoplankton biomass and therefore elevates
chlorophyll level in the central North Pacific. Increase in the modeled
chlorophyll expend the transitional zone and push the TZCF equatorward.
F. Chai1, M.-S. Jiang1, R. T. Barber2, R. A. Feely3, R. C. Dugdale4, T.-H. Peng5 and Y. Chao6
Modeled Decadal Variability of Primary Productivity and Air-Sea CO2 Flux in the Equatorial Pacific Ocean
1 School of Marine Science, 5471 Libby Hall, University of Maine, Orono, ME 04469
2 Duke University, NSOE Marine Laboratory, 135 Duke Marine Lab Road, Beaufort, NC 28516
3 Richard A. Feely (Ocean Climate Research Division, NOAA/PMEL, 7600 Sand Point Way NE, Seattle WA 98115
4 Romberg Tiburon Center, San Francisco State University, PO Box 855, Tiburon CA 94920
5 NOAA Atlantic Oceanographic and Meteorological Laboratory, Ocean Chemistry Division, 4301 Rickenbacker Causeway, Miami, FL 33149-1026
6 Jet Propulsion Laboratory, California Institute of Technology, 4800 Oak Grove Drive, Pasadena, CA 91109
ABSTRACT:
The response of primary production and sea-to-air
CO2 flux in the equatorial
Pacific to decadal timescale climate variability is investigated using a
physical-biogeochemical model forced with COADS wind stress and heat flux.
The circulation model resolves decadal variations over the past 40 years
with a decrease in the equatorward interior flow and a reduction of 20% in
the equatorial upwelling transport since 1976-77 climate shift. The decreased
volume transports causes a rise of sea surface temperature in the equatorial
upwelling zone by about 0.7°C since mid 1970s. Slowdown of the meridional
overturning and decrease of the equatorial upwelling transport have
significant impacts on marine ecosystem and carbon flux. The modeled primary
production and phytoplankton biomass decrease by 10% over the past 40 years
mainly due to reduction of upward nutrient flux. Our physical-biogeochemical
model results document that the equatorial Pacific sea-to-air
CO2 flux decreased by 20% after 1976-77
climate shift.
James Christian1 and Ricardo Letelier2
Modelling interannual variability of carbon fluxes at JGOFS Time-Series Station ALOHA
1 Earth System Science Interdisciplinary Center, University of Maryland
2 College of Oceanic and Atmospheric Sciences, Oregon State University
ABSTRACT:
The Hawaii Ocean Time-Series has collected one of the most complete data
sets on the temporal variability of dissolved and particulate carbon,
nitrogen and phosphorus for any location in the world ocean. To date
few prognostic ecosystem models have been coupled to models of carbon
chemistry and air-sea exchange, and most have considered only C and N,
and have employed fixed elemental (Redfield) ratios. We have developed
models for C-N-P stoichiometry that consider both inorganic and organic
dissolved pools, with fixed and variable ratios in phytoplankton biomass;
regeneration terms are common to both models. The results of these
models show that the biologically mediated oceanic sink for atmospheric
CO2 is consistently larger in the variable-ratio model. Interannual
variability of surface ocean dissolved inorganic carbon (DIC) is large
and is forced primarily by variability of precipitation. Covariance of
modelled and observed surface salinity and DIC suggest that the
precipitation fields generated by the Global Precipitation Climatology
Project are quite accurate at this location except during 1994-1995 when
precipitation appears to be substantially underestimated. The secular
trend in salinity-normalized DIC for 1988-2000 is
0.88 mmol m-3 y-1 in the upper 50 m,
consistent with observation-based estimates. This trend is primarily
caused by rising atmospheric CO2 although up to 25% may be attributable
to interannual variability in entrainment of subsurface water. The
range of DIC variability associated with variable freshwater flux is
about 100 times the annual accumulation, and there is an apparent
secular trend in total DIC that is about twice as large as the secular
trend in normalized DIC. This trend is due principally to declining
precipitation after 1998.
James Christian1 and Ragu Murtugudde1
Tropical Atlantic climate variability in a coupled physical-biogeochemical ocean model
1 Earth System Science Interdisciplinary Center, University of Maryland, College Park, College Park, MD, 20742
ABSTRACT:
A three-dimensional ocean biogeochemical model of the tropical Atlantic
Ocean was run for more than half a century (1949-2000) in order to
characterize the ocean biogeochemical response to variable forcing over
this period. The seasonal cycle in the equatorial upwelling zone agrees
reasonably well with observations and other published simulations but
underestimates phytoplankton biomass under strong upwelling conditions.
Away from the equator, nutrient flux and biological production are maximal
in each hemisphere's winter season, and appear to be proximately forced
by evapourative cooling and wind stirring rather than by Ekman upwelling.
The fraction of the total variance that is associated with the annual
cycle is considerably smaller for biogeochemical fields than for sea
surface temperature over this long simulation, and much of this variance
is associated with interdecadal changes. The tropical Atlantic appears
to have become more productive following the Pacific climate shift of
1976 and remained so until about 1989. Summer surface nitrate
concentrations during the 1990's were lower than those in the 1980's.
The relationship between the equatorial and off-equatorial regimes may
have changed following the 1976 event, with equatorial variability
dominating the basin-wide variance patterns after 1976.
S. Chung1, Kitack Lee1, C.L. Sabine2,3, R.A. Feely3, F.J. Millero4, R.M. Key5, and R. Wanninkhof6
Calcium Carbonate Budget in the Atlantic Ocean
1 SEE, Pohang University of Science and Technology, Pohang, Korea, email: ktl@postech.ac.kr
2 JISAO, University of Washington, Seattle
3 Pacific Marine Environmental Laboratory, NOAA, Seattle
4 RSMAS, University of Miami, Miami
5 AOSP, Princeton University, Princeton, New Jersey
6 Atlantic Oceanographic and Meteorological Laboratory, NOAA, Miami
ABSTRACT:
Several independent lines of recent evidence suggest that the dissolution
of calcium carbonate
(CaCO3)
particles is substantial in the upper ocean above the 100% calcite saturation
horizon. However, the direct evidence is not available and an underlying
mechanism remains unresolved. This shallow-water dissolution of carbonate
particles is in conflict with the long-held paradigm of the conservative
nature of pelagic
CaCO3
at shallow water depths. Here we used over 20,000 carbon measurements in
conjunction with CFC data from the WOCE/JGOFS global
CO2
survey to estimate the in-situ dissolution rates of
CaCO3
on isopycnal surfaces in the Atlantic Ocean. Dissolution in water depths above
the aragonite saturation horizon appears to be negligible. Much of dissolution
occurs in depths between the aragonite and calcite saturation horizons.
Dissolution rates north of 30°N are generally higher than the rates to
the south, which could be partially attributable to higher production of
CaCO3
in the North Atlantic than in the Atlantic side of the Southern Ocean: more
CaCO3
particles rain down; more particles are subjected to dissolution. The
total amount of
CaCO3
that is dissolved in the Atlantic Ocean was determined by integrating
estimated dissolution rates representing isopycnal surfaces throughout the
entire water column and correcting for alkalinity inputs from
CaCO3-rich
sediments. The basin-wide dissolution rate of
CaCO3
north of 30°S is approximately
0.21 Pg C yr-1,
which accounts for about 64% of the net
CaCO3
production for the same area. Our calculation using high quality water-column
inorganic carbon data provides the first basin-scale estimate of the
CaCO3
budget for the Atlantic Ocean, where the
CaCO3
production rate for a given area is the highest.
Robert Daniels1, Hugh Ducklow1, George A. Jackson2, Michael R. Roman3 and Tammi Richardson2
Plankton food web structure in the NABE region, May, 1989
1 School of Marine Sciences, The College of William and Mary, Gloucester
Point, VA 23062 bdaniels@vims.edu
2 Dept. of Oceanography, Texas A&M University, MS 3146, College Station,
TX 77843-3146
3 Horn Point Laboratory, P.O. Box 775, Cambridge, MD 21613
ABSTRACT:
We are investigating relationships between food web structure and
function across different oceanic biomes using an inverse method to
recover snapshots of food webs from sparse data. Specifically, we
focus on how food web structure, as defined by the relative magnitude
of C and N flows in a generic food web, influences particle export,
nutrient regeneration, and dissolved organic carbon (DOC) cycling.
Our model food web includes large and small phytoplankton, meso-and
microzooplankton, bacteria, dissolved and particulate detritus, ammonium
and nitrate. The majority of flows in food webs are unknown quantities
that leave many questions about food web function. The inverse method,
first used on plankton food webs by Vezina and Platt (1989) is a least
squares approach of recovering flows from plankton food webs for which
few observed data exist. The inverse method provides a solution that
is consistent with the observations and with biological constraints
set forth in the model. Our poster presents results of an inverse
solution for a North Atlantic food web using data from the NABE (North
Atlantic Bloom Experiment) study. The plankton food web was recovered
for both carbon and nitrogen constituents in separate solutions.
Analysis of the inverse solution shows that microzooplankton dominated
the processing of carbon in the system, including grazing of phytoplankton
and contributions to the DOC pool. Bacteria were very active, consuming
DOC equivalent to about 60% of the net primary production. Also,
the mesozooplankton export of carbon through direct fecal pellet sinking
contributed to only 1% of the export.
D. DeMaster1, C. Thomas1, M. Alperin2, L. Mayer3, M. Green4, J. Aller5, R. Aller5, C. Martens2, N. Blair1, L. Benninger6 and R. Jahnke7
Studies of Organic Carbon Deposition, Recycling, and Burial on the Continental Margin Off Cape Hatteras, NC: The Ocean Margins Program
1 Dept. of Marine, Earth, and Atmospheric Sciences, No. Carolina State University, Raleigh, NC 27695
2 Dept. of Marine Sciences, University of No. Carolina, Chapel Hill, NC 27599
3 Darling Marine Center, University of Maine, Walpole, ME 04573
4 Dept. of Marine and Environmental Science, St. Josephs College, Standish, ME 04084
5 Marine Sciences Research Center, State University of New York, Stony Brook, NY 11794-5000
6 Dept. of Geology, University of No. Carolina, Chapel Hill, NC 27599
7 Skidaway Institute of Oceanography, Savannah, Georgia 31411
ABSTRACT:
As part of the Ocean Margin Project, the nature and fate of organic
matter reaching the continental margin seafloor off Cape Hatteras,
NC has been studied.
The deposition rate (or rain rate) of organic carbon to this area ranges from 3-12
moles C m-2 yr-1.
Based on stable and radioactive carbon budgets, nearly all of the organic carbon is
of marine origin and plankton make up from 0-30% of the organic C
reaching the seafloor. Older marine organic matter that has been
reworked and laterally advected to the margin comprises 60-90% of
the organic carbon flux to the seafloor, whereas a refractory organic
carbon source contributes 10-15%. The abundances of benthic macrofauna
in continental margin sediments correlate with POC rain rate when
the OMP data are combined with broader regional studies off North
Carolina.
The organic carbon content of the surface sediments on the upper continental slope off Cape Hatteras ranges from 1.0 to 3.5 wt. %. These fine-grained sediments have a surface area ranging from 3 to 25 m2 g-1. Sedimentary organic carbon contents increase as grain size decreases (with water depth a secondary control). The organic loadings on surfaces of lithogenic sediment (1.5-4.5 mg OC m-2) are some of the highest measured in continental margin sediments under an oxygenated water column. Despite these high organic loadings, the mineral surfaces are essentially bare of organic coatings. High levels of dissolved organic carbon (DOC) in OMP study area pore waters appear to have little effect on the organic loading of the slope sediments. Estimates of organic carbon production by benthic fauna suggest that bacterial carbon fixation and macrofaunal carbon fixation occur at comparable rates for water depths greater than 500m. However, at depths less than 500m, where there are higher abundances of bacteria, microbial fixation rates may exceed the macrofaunal rates by a factor of 3 fold or more. The enriched D14C contents of benthic fauna from the OMP study area indicate that bomb 14C is not only making it to the seafloor, but is the predominant source of nutrition for the benthic food web. Based on 14C mass budget calculations for surface sediments, the organic matter tagged with bomb 14C comprises only a few tenths of a percent of the total organic carbon in near-interface deposits.
Bioirrigation can occur to depths as great as 200 cm (commonly 60-100 cm) in these continental margin deposits of North Carolina. The bioirrigation fluxes of dissolved inorganic carbon out of the seabed range from 2.9-7.8 moles C m-2 y-1, whereas benthic lander flux chamber experiments (with limited or no bioirrigation) yield values between 1 and 4 moles C m-2 y-1. Bromide incubation experiments on board ship corroborate the rapid transport of overlying water down into the sediment column. The penetration depths for bromide were as great as 7 cm over a period of 24 hours with the mean bromide penetration rates suggesting transport more than an order of magnitude greater than molecular diffusion.
Distributions of 234Th and chlorophyll suggest that these continental margin sediments are intensely bioturbated in the upper 7 cm over a time scale of weeks to months (Db values range from 1-200 cm2 y-1). On a 50-100 year time scale, Pu and 210Pb distributions suggest that the upper 10 to 27 cm of the sediment column are mixed more slowly (Db values ranging from 0.3 to 5.2 cm2 y-1). Burial rates of organic carbon were estimated from seabed organic carbon profiles and the distributions of Pu and 210Pb (0.1-4.7 mole C m-2 y-1 on a hundred-year time scale) as well as 14C (0.02-1.7 mole C m-2 y-1 on a thousand-year time scale). Relative to the deposition rate, the seabed preservation efficiency ranges from 3-40% (mean ~15%) with little systematic down-slope variation. In these deposits a relatively high amount of remineralized nitrogen (~68%) ultimately becomes denitrified. Burial of organic carbon in slope sediments (average rate of 0.7 moles of C m-2 y-1) accounts for only 5% of the primary production in the overlying water. Considering production and burial on the continental shelf and slope as a whole, the accumulation of organic matter on the upper slope only accounts for 0.6% of the primary production in the shelf/slope system. Despite the fact that the Ocean Margins Project site was selected to maximize the offshore transport and deposition of organic carbon, burial of organic matter in North Carolina slope sediments is not a major sink for primary production occurring in this continental margin system.
Curtis Deutsch1, John Dunne1, Jorge Sarmiento1 and Nicolas Gruber2
Diagnosing Global Oceanic Nitrogen Fixation and Denitrification
1 Atmospheric and Oceanic Sciences Program, Princeton Univ., P.O. Box CN710, Princeton, NJ 08544-0710, USA
3 Inst. Geophysics and Planetary Physics & Dept Atmos. Sci., UCLA, Los Angel
es, CA 90095-1567
ABSTRACT:
We present results from diagnostic simulations of the global ocean
nitrogen cycle including Nitrogen Fixation and Denitrification fluxes.
We begin with a simple ecosystem model in which 2 size classes of
phytoplankton produce particulate and dissolved organic matter with a
prognostic f-ratio. Organic matter export occurs according to a ballast
based remineralization scheme after Armstrong et al. Simple
parameterizations are added for nitrogen fixation and denitrification,
based on local N:P stoichiometry and O2
concentration respectively. We
find that total water column denitrification is too large by a factor of 2
due to extensive model anoxia. Patterns of nitrogen fixation show most new
nitrate the be added in the subtropical gyres of the Pacific. Finally,
nutrient uptake ratios diagnosed by the model also suggest that the
Southern Ocean is a region of low N:P uptake.
Michael S. Dinniman1, John M. Klinck1 and Walker O. Smith, Jr.2
A Model Study of Circulation and Biogeochemical Processes in the Ross Sea
1 Center for Coastal Physical Oceanography, Old Dominion University, Norfolk, VA 23529 msd@ccpo.odu.edu
2 Virginia Institute of Marine Sciences, College of William and Mary, Gloucester Point, VA 23062 wos@vims.edu
ABSTRACT:
Physical forcing, which includes advective circulation, vertical mixing,
and vertical stratification, may be the primary factor producing the
observed vertical and horizontal variability in phytoplankton distribution
and primary production in the Ross Sea. Related to this, exchange of
Circumpolar Deep Water (CDW) onto Antarctic Seas and continental shelves
has a large influence on sea ice and biological processes. As part of the
US JGOFS Synthesis and Modeling effort, we are investigating circulation
and nutrient transport in the Ross Sea with an eddy permitting, regional,
3D, numerical circulation model. The present effort focuses on
implementation and testing of the circulation model. Later work will
consider more realistic biogeochemical processes.
We use the Rutgers/UCLA Regional Ocean Model System. Initial model
fields of temperature and salinity are derived from the World Ocean Atlas
(WOA98). Two different wind stress products, a monthly climatology and daily
values (August 1996 to July 1997), are applied to the model. Instead of
using a fully dynamic sea-ice model, ice concentrations are specified using
the SSM/I climatology and this, along with the COARE bulk flux algorithm,
is used to compute the model surface heat and salt fluxes. Vertical mixing
in the interior and surface boundary layer is done using the K profile
parameter (KPP) vertical mixing scheme (modified for the presence of ice).
A radiation boundary condition is used on all the open boundaries along with
adaptive nudging to monthly climatologies of tracers and volume transport.
The effects of the Ross Ice Shelf are modeled by relaxing the temperature
and salinity to climatological values along the edge of the shelf. Model
circulation is strongly affected by bottom topography, due to weak
stratification, and agrees with schematics of the general flow and long-term
current measurements except near the southern boundary. There is about 2 Sv.
of CDW transported onto the shelf and much of the cross shelf break transport
is confined to small sections that are determined by bathymetry. The
seasonal variation of the depth and temperature of the model mixed layer also
match observations reasonably well.
Hugh Ducklow1, Davey Siegel2 and Bob Key3
How is SMP Doing? Perspectives on observational syntheses.
1 School of Marine Sciences, The College of William and Mary, Gloucester
Point, VA 23062
2 Institute for Computational Earth System Science, University of California, Santa Barbara, Santa Barbara, CA
3 AOSP, Princeton University, Princeton, New Jersey
ABSTRACT:
US JGOFS and its supporting funding agencies set an important precedent
for the ocean sciences in 1996 by initiating a major program aimed at
synthesizing data and understanding gained during the field phases of JGOFS.
There had been smaller post-field synthesis projects funded previously but
nothing on the scale of JGOFS had been attempted. The SMP was conceived
as a full-fledged science program, equivalent in size, cost and scope
to a major process study. In fact, the implementation process was
conceived in an analogous way to a process study. Individual elements
necessary for successful achievement of program goals were identified in
announcements of opportunity and proposals were submitted in response.
A coordinated program was composed of successful PI's. This process
isn't fool-proof. Some desired projects were never proposed or funded,
but some unexpected ones came along as well. As we near the final stage
of SMP there have been several iterations of announcement and response,
and about half the funded projects have been completed. This is a good
point to ask how SMP is doing and if we have met the goals we set; and
especially, to take a look at the science it has produced.
A scan through the US GOFS Blue Book (NAS, 1984) is surprising from the
vantage of SMP, 16 years after the program was first imagined. Plans at
the time emphasized remote sensing, primary production measurements and
sediment traps. There was little explicit discussion of carbon, nor much
on modeling. CO2 was nearly absent. Of course it is not surprising that
the program grew and changed over 2 decades in ways few expected. Still
it is instructive to look at what SMP has done to wrap up JGOFS, both
as it was originally designed, and in what it became. Here, we look in
particular at 3 key elements of the overall program: remote sensing, the
CO2 survey, and new production/export studies, drawing mostly on
completed SMP projects. A accompanying talk on modeling and prediction
by Sarmiento & Dunne expands on our look at SMP.
J. P. Dunne1, R. A. Armstrong2, C. A. Deutsch1, A. Gnanadesikan1, N. Gruber3, J. L. Sarmiento1 and P. S. Swathi1
Development of a global, multi-element biogeochemical model: description, calibration and comparison with ocean color
1 Atmospheric and Oceanic Sciences Program, Princeton
Univ., P.O. Box CN710, Princeton, NJ 08544-0710, USA
2 Marine Sci. Res. Ctr, SUNY, Stony Brook, NY 11794-5000
3 Inst. Geophysics and Planetary Physics & Dept Atmos. Sci., UCLA, Los Angel
es, CA 90095-1567
ABSTRACT:
We have developed a model to simulate ecosystem dynamics relating to
regenerated production, sinking particle export and transport of dissolved
organic matter in the global ocean. A key feature of this model is a
representation of grazing that reproduces observed allometric
relationships between large and small phytoplankton. We present an
extensive compilation of data on primary production and particle export,
and use this data to calibrate this relatively simple, highly
parameterized model of particle export and remineralization. Production
is determined by forcing nutrients toward observations. Regeneration is
described as a function of temperature and community structure, competing
with the sinking of detrital material through the water column. Detrital
sinking is described as a function of mineral ballast. Dissolved organic
matter production is described as a function of phytoplankton production
and nutrient limitation and calibrated to survey data. The resulting
model has been incorporated into the Princeton Ocean Biogeochemical Model
to diagnose global primary production, new production, particle export and
dissolved organic matter transport. Model results are compared with
satellite-based primary production from ocean color to provide insights
into deficiencies in the model physics and biology as well as point to
potential deficiencies in the Satellite estimates.
General principles of marine food web structure in relation to export production
1 Institute of Marine and Coastal Science, Rutgers University, New Brunswick, NJ 08901 falko@imcs.rutgers.edu
ABSTRACT:
Over the past decade, significant progress has been made in integrating
measurements and models of oceanic net primary production, such that
independent estimates of global carbon fixation have converged to within
approximately 10% of the mean. While still far from perfect, the
uncertainties in NPP are far smaller than those derived for export
production. A major problem in understanding export fluxes is the
application of NPZ models, that are inherently difficult to parameterize.
Here I suggest that simple estimates of upper ocean mixing rates and mixed
layer depths can be used to derive a latitude-dependent size structure for
phytoplankton, that can, in turn, be use to constrain both estimates of export
production and food web structure. Global climatologies of the particle size
spectrum, in conjunction with simple models of phytoplankton functional groups,
should help gain insight into herbivour community structure and food web
efficiency.
R.A. Feely1, C.L. Sabine2, J.L. Bullister1 and D. Greeley1
Organic carbon remineralization rates in the Pacific Ocean
1 NOAA/Pacific Marine Environmental Laboratory; Seattle, USA
2 University of Washington/JISAO, Seattle, USA
ABSTRACT:
As a part of the U.S. JGOFS synthesis and modeling project, researchers have
been working to synthesize the WOCE/JGOFS/DOE/NOAA global
CO2 survey data to
better understand carbon cycling processes in the oceans. Working with
international investigators we have compiled a Pacific Ocean data set with over
35,000 unique sample locations analyzed for at least two carbon species,
oxygen, nutrient, CFC tracers, and hydrographic parameters. These data are
being used determine the rates of in-situ organic carbon remineralization
within the water column of the Pacific Ocean. Organic carbon remineralization
rates (ranging from about 0.1 - 11 µmol kg-1 yr-1) are observed in the upper
water masses from about 100 - 500 m. The rates are generally highest just below
the euphotic zone and decrease with depth to values that are low and constant
in the Circumpolar Deep Water. Within the North Pacific Intermediate Water
(depth range: 400 - 800 m), organic carbon remineralization rates are more than
10 times higher than those observed in deepwater depths (average = 0.042 µmol
kg-1 yr-1) of the Pacific Ocean.
Katja Fennel1, Mark Abbott1, Yvette Spitz1, Jim Richman1 and David Nelson1
Modeling Controls of Phytoplankton Production in the Southern Ocean -- Modern and Glacial Scenarios
1 College of Oceanic and Atmospheric Sciences Oregon State University 104 Ocean Admin. Bldg. Corvallis, Or 97331
ABSTRACT:
To elucidate controls of primary and export production in the Southern
Ocean we developed a one-dimensional physical/biological model. The model
is applied to four stations in the southwest Pacific sector spanning the
Subantarctic Zone, the Polar Front, and the Seasonal Ice Zone. The biological
model component tracks the elemental cycles of nitrogen and silica. Diatoms
are represented as a separate functional group. Small phytoplankton and
zooplankton are tightly coupled. The one-dimensional model cannot explicitly
represent horizontal fluxes of heat, freshwater and nutrients. Since these
fluxes are important, we restore the temperature, salinity and nutrients
in the model to available observations. We use two different approaches
to include the effect of low iron availability. In modern ocean simulations,
iron availability is taken into account implicitly by typical phytoplankton
growth rates and a typical Si:N cell quota of diatoms. In other modern
and glacial simulations, iron is included semi-explicitly, that is, iron
modulates the photosynthetic efficiency and is taken up during phytoplankton
growth but not tracked in the pelagic system. The model captures the essential
features of the different zonal subsystems. "Top-down" control of small
phytoplankton by intense grazing and "bottom-up" control of diatoms by
light and silicic acid supply are the main factors for the simulated behavior.
In simulations of glacial scenarios -- assuming an increase in available
iron -- primary and export production increase, in particular if we assume
an acclimation of the Si:N cell quota of diatoms in response to the higher
iron levels.
Changes in productivity, nutrient utilization and hydrology in the Southern Ocean during the last glacial maximum and its potential impact on atmospheric CO2
1 Woods Hole Oceanographic Inst., Woods Hole, MA
ABSTRACT:
Following R. F. Anderson's overview of the results from the AESOPS program,
I will try to synthesize the results from paleoceanographic research
conducted in the southern ocean, and discuss the possible role of the
biological pump of this region in controlling atmospheric CO2 on glacial
to interglacial timescale. The goal will be to generate a discussion on
possible new insights that the recent results from the southern ocean
JGOFS program may provide to better constrain our evolving interpretation
of the sedimentary record.
Marjorie A. M. Friedrichs1, Jerry Wiggert2 and Raleigh Hood3
Preliminary results from the Regional Ecosystem Modeling Testbed Project: The Arabian Sea
1 Center for Coastal Physical Oceanography, Old Dominion University, Norfolk, VA 23529
2 ESSIC, University of Maryland, College Park, MD 20742
3 University of Maryland Center for Environmental Science, Cambridge, MD 21613
ABSTRACT:
The primary objective of the Regional Testbed Project is to
quantitatively compare the different regional models that have been
developed as part of the JGOFS SMP, in order to critically examine which
ecosystem structures and model formulations are best able to
simulate observed biogeochemical cycling in specific regions as well as
simultaneously in multiple regions. In order to
facilitate these intercomparisons we are developing a set of regional
testbeds, each of which will contain one-dimensional physical forcing fields
from either 3D physical model output or data, as well as biogeochemical data
for either assimilation or evaluation. By running various ecosystem models
using the same physical forcing, and evaluating them using the same
biogeochemical data, we can objectively compare different ecosystem models
and modeling approaches.
In the first year of this project, we have concentrated on formulating a
prototype testbed in the Arabian Sea. In this testbed we have three distinct
marine ecosystem models with varying levels of complexity, including a
four-component model with diatom-like phytoplankton growth, a five-component
model emphasizing the microbial loop, and an eight-component model
containing multiple plankton size classes. The models are applied within a
consistent one-dimensional framework at the site of the WHOI mooring (15.5°N,
61.5°E), using physical forcing fields obtained from the mooring
data when possible, as well as from two three-dimensional circulation
models. Chlorophyll a, nutrient and sediment trap data are assimilated using
the variational adjoint method. After objectively optimizing each model in
this manner, we quantitatively compare the performance of the different
models to assess which model formulations best represent the fundamental
underlying biogeochemical processes and capture the magnitude and
variability of observed biogeochemical quantities.
Dave M. Glover1 and Maureen H. Conte1
A Coupled Epipelagic-Meso/Bathypelagic Particle Flux Model for the Bermuda Atlantic Time-series Station (BATS)/Oceanic Flux Program (OFP) Site: Phase 1, the Ecosystem Kernel
1 Dept. of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, MA 02543 dglover@whoi.edu mconte@whoi.edu
ABSTRACT:
The overarching goal of this project is to mechanistically connect
euphotic zone processes with meso- and bathypelagic zone processes. It
is our long term goal to accomplish this by means of a prognostic model
that can be used to further our understanding of unparalleled
time-series of deep-water sediment traps (21+ years) at the Oceanic
Flux Program (OFP), euphotic zone measurements (10+ years) at the
Bermuda Atlantic Time-series Site (BATS). In order to realize this
goal we will derive a meso/bathypelagic ecosystem structure and use it
to model the flux of biogeochemically active constituents (carbon,
nitrogen and silica) through the water column. In this initial phase,
we present the kernel of the mesopelagic ecosystem in a
zero-dimensional, nitrogen only form. The equations and initial
parameters are presented along with insight as to how this kernel fits
into the over all scheme.
Nicolas Gruber1, Jim Orr2 and OCMIP-members, Chris Sabine3 and GLODAP members, Manuel Gloor4 and Jorge Sarmiento5
The oceanic sink for anthropogenic CO2: Combining observations with models
1 Institute of Geophysics and Planetary Physics & Department of Atmospheric Sciences, UCLA, Los Angeles, CA.
2 Laboratoire des Sciences du Climat et de l'Environnement CEA Saclay, Gif-sur-Yvette, France.
3 NOAA Pacific Marine Environmental Laboratory, Seattle, WA.
4 Max Planck Institute for Biogeochemistry, Jena, Germany.
5 AOS Program, Princeton University, Princeton, NJ.
ABSTRACT:
While much progress has been made in constraining the global-scale uptake
of anthropogenic CO2 by the ocean, the spatial pattern of this uptake flux
is not well known. This is to a large degree due to the fact that the flux
of anthropogenic CO2 across the air-sea interface cannot be separated from
the often much larger air-sea flux of natural CO2. However, several
independent methods have been developed over the last few years to identify
the amount of total anthropogenic CO2 in ocean water as well as how this
concentration changes over time (see abstract by Sabine et al.). But
relating an observed accumulation of anthropogenic CO2 in the water column
to an anthropogenic CO2 uptake flux at the sea surface is not
straightforward, since this requires a detailed knowledge of how the
large-scale circulation connects the surface ocean with the ocean's
interior. I present and discuss two model-based approaches that attempt to
establish this connection and thereby constrain the regional air-sea fluxes
of anthropogenic CO2. The first approach is the traditional method of
comparing results from forward ocean carbon model simulations with ocean
reconstructions of anthropogenic CO2 and then, given reasonable agreement
between the model simulated and the observed fields, arguing that the model
simulated air-sea fluxes of anthropogenic CO2 are realistic. I will follow
this approach using results from the recently completed 2nd phase of the
Ocean Carbon-cycle Model Intercomparison Project (OCMIP). Since 13 global
models provided output for anthropogenic CO2, it becomes feasible to bound
the observed concentration fields with the modeled ones, thereby providing
support for the argument that the real fluxes will lie within the range of
the modeled ones. The second approach is a formal inversion method on the
basis of Green's functions, whereby the magnitude of concentration patterns
created by emitting dye tracers from a few pre-determined regions are
linearly combined in such a manner that they agree with the observations
optimally (in the least squares sense). Despite fundamental differences in
the two methods, similar results emerge. Forward and inverse models
indicate that the ocean south of 36°S takes up about 40% of the global
anthropogenic CO2 uptake. The second most important region for uptake are
the tropics, followed by the North Atlantic. Despite agreements in these
overall pattern, substantial differences exist at more regional scales.
Nicolas Gruber1, Holger Brix1, Charles D. Keeling2 and Nicholas Bates3
Interannual to decadal variability in the carbon cycle of the subtropical gyres: A comparative study between Station 'S'/BATS and HOT
1 IGPP and Dept. of Atmospheric Sciences, UCLA, Los Angeles, CA 90095
2 Scripps Institution of Oceanography, UCSD, La Jolla, CA
3 Bermuda Biological Station for Research, Inc., Bermuda
ABSTRACT:
We examine interannual to decadal variability in the ocean carbon cycle in
the subtropical gyres on the basis of two long-term upper ocean time-series
records. The longest record exists from near Bermuda, where sampling was
initiated in late 1983 at Station 'S' and later expanded to cover the
Bermuda Atlantic Time-series Station (BATS) site as well. The second
record stems from the ALOHA site near Hawaii, where sampling was started
with the establishment of the Hawaii Ocean Time-series (HOT) program in
1988. Both sites exhibit substantial interannual variability in all
measured and computed carbon properties (dissolved inorganic carbon (DIC),
total alkalinity (Alk), computed ocean surface partial pressure of CO2
(pCO2), and the 13C/12C ratio of DIC). We also find a strong
anti-correlation between sea-surface temperature (SST) anomalies and DIC
anomalies at both sites, which leads to a suppression of the correlation of
either of these properties with pCO2. We employ a slightly modified
version of the diagnostic box model of Gruber et al. [1998] to quantify
the contribution of the processes controlling the carbon cycle variability
at these two sites. Near Bermuda, the variability is largely driven by
variations in winter mixed layer depths, which impact both the amount of
DIC that gets entrained into the mixed layer and the magnitude of net
community production. The variability of air-sea CO2 fluxes tends to be
controlled by sea-surface temperature (SST) anomalies and accompanying
wind-speed anomalies with larger CO2 uptake from the atmosphere during
years of deeper than normal mixed layers. We find significant correlation
of the magnitude of net community production and air-sea CO2 fluxes with
the North Atlantic Oscillation (NAO), attributed to a strong influence of
the NAO on convection and SST during winter. Our diagnostic analyses of
the HOT data indicate a more complicated relationship between the
variability in physical forcing and the response of the surface ocean
carbon cycle. This is likely caused by a much weaker role played by mixed
layer variations. As was the case near Bermuda, interannual variability in
air-sea gas exchange is primarily controlled by variations in SST and its
often associated changes in windspeed. By contrast, interannual variations
in net community production are largely independent of changes in local
physical forcing. Rather, we find that variability in net community
production is associated with changes in horizontal advection, a process
that appears to play a more important role near Hawaii than near Bermuda.
This might suggest that a significant fraction of the limiting nutrient
supply near Hawaii is supplied laterally rather than vertically.
Nicolas Gruber1, Hartmut Frenzel1, Patrick Marchesiello1 and J.C. McWilliams1
On the role of transport in decoupling export from new production
1 IGPP and Dept. of Atmospheric Sciences, UCLA, Los Angeles, CA 90095
ABSTRACT:
One of the most important paradigms that guided the biological
oceanographic community during the JGOFS period is that new production can
be numerically equated with export production in steady-state situations.
This permitted us to use estimates of new production as a substitute for
the often more difficult measurements of export production. The assumption
underlying this paradigm is that horizontal transport of organic nitrogen
is neglible relative to vertical export. We investigate here the validity
of this assumption using an eddy-resolving coupled physical-biological
model of the central Californian coast. This system is dominated by strong
coastal upwelling and generic instability of the flow regime, leading to
intense formation of eddies and other meso-scale and submeso-scale
features, such as jets and squirts. We find that the horizontal and
vertical transports associated with such circulation structures lead to a
substantial decoupling of new and export production. New production shows
the expected on-offshore gradient and is primarily determined by the
vertical supply of nitrate. By contrast, export production shows a
complicated pattern with both negative and positive values, determined
primarily by the convergence and divergence of the flow and the associated
vertical transports in and out of the euphotic zone. These annual mean
divergences and convergences are associated with the fact that eddies and
other meso-scale features are not entirely randomly distributed, but set up
an eddy-induced mean transport. Our results indicate therefore that the
paradigm of numerically equal new and export production has to be used with
great care, particularly in dynamic oceanographic environments.
Raleigh R. Hood1, Kevin E. Kohler2, Julian P. McCreary, Jr.3 and Sharon L. Smith4
A 4-Dimensional Validation of a Coupled Physical-Biological Model of the Arabian Sea
1 University of Maryland Center for Environmental Science, Cambridge,
Maryland
2 Oceanographic Center, Nova Southeastern University, Dania, Florida
3 International Pacific Research Center, University of Hawaii, Honolulu,
Hawaii
4 Rosenstiel School of Marine and Atmospheric Science, University of Miami,
Miami, Florida
ABSTRACT:
In this paper, we use a coupled biological/physical model to synthesize
and understand observations taken during the US JGOFS Arabian Sea
Process Study (ASPS). Its physical component is a variable-density,
4 and 1/2 layer model; its biological component consists of a set
of advective-diffusive equations in each layer that determine nitrogen
concentrations in four compartments, namely, nutrients, phytoplankton,
zooplankton, and detritus. Solutions are compared to horizontal
sections and time series from the ASPS data set, including observations
of mixed-layer thickness, chlorophyll concentrations, inorganic
nitrogen concentrations, zooplankton biomass, and particulate nitrogen
export flux. Through these comparisons, we adjust model parameters to
obtain a "best-fit", main run solution, identify key biological and
physical processes, and identify model strengths and weaknesses.
Substantial improvements in the agreement between the model and the
observations are obtained by: 1) adjusting the turbulence-production
coefficients in the mixed layer model to reduce bouyancy mixing; 2)
changing the sinking rate and remineralization rate of detritus to to
provide more rapid export and increase flux; and 3) introducing a
parameterization of particle aggregation to lower phytoplankton
concentrations in coastal upwelling regions. With these adjustments
the model captures many key aspects of the observed physical and
biogeochemical variability in the Arabian Sea. Successes include good
agreement between the modeled and observed DIN concentrations and
reproduction of much of the temporal and spatial variability in the
mixed layer depth and phytoplankton concentrations. In addition, the
model-estimated zooplankton concentrations agree with the observed
mesozooplankton concentrations in offshore waters, and the model
captures seasonal and spatial changes in the export flux remarkably
well. Nonetheless, there are significant differences between the
modeled and observed phytoplankton concentrations on virtually every
cruise. In some cases these can be attributed to problems with the
model's representation of the MLD variability, while in others they can
be related to differences in the spatial extent of coastal upwelling,
or differences in the timing of blooms between the model and the
observations. Still other discrepancies can be attributed to the
absence of mesoscale eddies and filaments in our relatively low
resolution model. Although some problems do appear to be related to
biological model, such as overestimation of phytoplankton
concentrations due to underestimation of zooplankton grazing losses
near the coast, we conclude that future efforts to improve the model
should be focused primarily on increasing the resolution of physical
model so that it can capture more of the observed mesoscale
variability.
Andrew J. Irwin1 and Paul Falkowski1
Predicting Chlorophyll from Satellite and Climatological Data Products
1 Institute of Marine and Coastal Sciences, Rutgers University
ABSTRACT:
An important goal in the current synthesis and modeling phase of the
JGOFS project is to be able to identify the functional groups responsible
for phytoplankton blooms. Some phytoplankton groups (coccolithophorids,
Trichodesmium spp.) have distinct optical signatures that can be detected
from space. Diatoms, the most productive of the functional groups are
not uniquely identifiable on the basis of their optical characteristics.
We attempt to identify diatoms using unique signatures from satellite and
climatological data such as nitrate:silicate ratios. Many data sources
are available including irradiance, sea surface temperature, surface wind
speeds (all from satellites and with high spatial and temporal
resolution), nitrate, phosphate, and silicate concentrations, upwelling
velocities, mixed layer depth, aeolian dust input, and salinity (data or
models, with generally poor spatial and temporal resolution). As a first
step we construct a statistical model to predict chlorophyll
concentration. Our best model uses 7 predictors: sea surface
temperature, irradiance, irradiance / mixed layer depth, nitrate,
upwelling velocity, ocean depth, and salinity. These results capture many
of the spatial and temporal features of chlorophyll blooms. The model
accounts for 65% of the variability in log chlorophyll and the
predictions have an RMS error of 0.23 (log chlorophyll concentration).
Using an increase in the derivative of the nitrate:silicate ratio as an
indicator of diatoms, we estimate that 46% of chlorophyll is associated
with diatoms.
Andrew J. Irwin1, Stew Sutherland2, Taro Takahashi2 and Paul Falkowski1
Using primary productivity to improve predictions of pCO2
1 Institute of Marine and Coastal Sciences, Rutgers University
2 Lamont-Doherty Earth Observatory, Columbia University
ABSTRACT:
abstract
The CO2 flux across the air-seawater boundary is the product of the
difference in the partial pressures of CO2 and the gas exchange
coefficient. Annual fluctuations in pCO2 in the ocean are driven by sea
surface temperature (SST), physical mixing, and biological activity.
Previous models using SST have been able to produce detailed maps of pCO2
in the surface ocean and have been used to estimate CO2 fluxes. Analysis
of these models shows that the unexplained variation in pCO2 is
correlated with biological activity. A statistical model using SeaWiFS
chlorophyll, temperature, irradiance, and mixed layer depth is able to
predict much of the residual variation in pCO2. Incorporating this
biological information reduces the RMS error in pCO2 from 17 uatm to 13
umatm in the North Pacific.
M.-S. Jiang1, F. Chai1, R.C. Dugdale2, F.P. Wilkerson2, T.-H. Peng3 and R.T. Barber4
A nitrate and silicate budget in the equatorial Pacific Ocean: A coupled biological-physical model study
1 School of Marine Sciences, 5471 Libby Hall, University of Maine,
Orono, ME 04469
2 Romberg Tiburon Center, San Francisco State University, 3152 Paradise
Drive, Tiburon, CA 94920
3 NOAA Atlantic Oceanographic and Meteorological Laboratory, Ocean
Chemistry Division, 4301 Rickenbacker Causeway, Miami, FL 33149-1026
4 NSOE Marine Laboratory, Duke University, 135 Duke Marine Lab Road,
Beaufort, NC 28516
ABSTRACT:
A coupled biological-physical model is developed to simulate the low
silicate, high nitrate low chlorophyll (LSHNLC) condition in the equatorial
Pacific Ocean. A detailed budget in the Wyrtki Box (5°N-5°S,
180°W-90°W)
is carried out to understand the major sources and cycling of nitrogen
and silicon in the equatorial Pacific. The modeled mean new and primary
production compare well with previous observed and modeled estimates.
As a major source of nutrients to the equatorial Pacific, the Equatorial
Undercurrent provides slightly more nitrate than silicate to the upwelling
zone, which is defined as (2.5°N-2.5°S, 180°-90°W).
On the other hand,
the nitrogen recycling is relatively more efficient than biogenic
silicon. As a result of these combined effects, the physical supplies
of silicate and nitrate into the euphotic depth in Wyrtki Box have
a ratio about 0.85 (2.5 vs. 2.96 mmol/m2/day).
Silicate and nitrate are taken up with a ratio of 1.17
(2.72 vs. 2.33 mmol/m2/day) within
euphotic zone. The ratio of biogenic silica and nitrogen export production
at the base of euphotic zone follows a 1.1:1 ratio. In the central
equatorial Pacific, low silicate concentration limits diatom growth,
therefore non-diatom new production accounts for most of the new production.
Slightly higher silicate supply in the east maintains elevated diatom
growth rate and new production associated with diatom tends to be
higher. The new production associated with small phytoplankton is
nearly constant along the equator. The nitrate and silicate budget
calculation suggests a potential role of silicate regulation on the
new production and carbon cycle in this area.
Deep secrets from the marine food web
1 School of Ocean and Earth Science and Technology, University of Hawaii, Honolulu, HI 96822
ABSTRACT:
For more than a century, oceanographers have studied the interactions
between the photosynthetic production of organic matter and nutrient
dynamics in the sea. This research has been field-oriented and
transdisciplinary, occurring at the intersections of research in
microbiology, physics, analytical chemistry, cell physiology and ecology.
The global data base derived from this collective effort established a
sound scientific understanding of nutrient dynamics and the vital role of
microorganisms, both autotrophic and heterotrophic, in the coupled organic
matter production and decomposition cycles in the sea. However, novel
approaches employed over the past two decades, including new designs in
field experiments, repeat field observations and remote sensing capabilities,
and updated methods of sample analysis, have led to a revolution in our
thinking about the mechanisms and controls of nutrient dynamics in
mare incognita, the hidden sea. Contemporary paradigms bear
only partial resemblance to the dogma of the past, and are likely to
evolve further as new data and new ideas are presented for open discussion
and debate.
R.S. Lampitt1, E.E. Popova1 and I.J. Totterdell1
Downward particle flux estimates from models and measurements: The global perspective
1 Southampton Oceanography Centre, Empress Dock, Southampton, SO14 3ZH, UK R.Lampitt@soc.soton.ac.uk
ABSTRACT:
Variability in upper ocean biogeochemistry determines to a large degree the
temporal and spatial variations in the deep ocean downward flux of
particulate material. The relevant upper ocean processes can be described by
a variety of modelling approaches from simple 1D to those that are embedded
in powerful general circulation models of the oceans. We describe results from
a one dimensional upper ocean model at a location near to the NABE site in
the Northeast Atlantic. This model is driven by meteorology to predict export
flux and from that to provide a measure of downward flux at 3000m over a ten
year period. The results have been found to compare very favourably with
measured flux at this depth using sediment traps in terms of both the general
magnitude and the characteristics of seasonal variation.
We then describe results from two similar ecosystem models that have been
embedded into two general circulation models (HADOM3L and OCCAM). Both are
Bryan-Cox based level models, the most important difference between them
being the level of spatial resolution. The ecosystem models are of similar
complexity. They have been used to derive global patterns of downward flux of
organic carbon at 2000m and we compare the model outputs with each other. At
41 specific locations where long term high quality sediment trap data are
available, we compare the outputs from the models with measured data. The
quality of agreement between the various approaches is sometimes good but is
also very variable and the reasons for this variability are discussed.
Simple solutions to complex problems
1 University of Hawaii, Oceanography Dept., Honolulu, HI 96822
ABSTRACT:
Virtually all mathematical models that describe the population dynamics
of aquatic food webs involve nonlinear relationships between the
concentration of prey or substrate and the growth rate of the consumer.
The nonlinearity is typically captured in a mathematical expression that
involves the concentration of the prey or substrate and a single
constant such as the half-saturation constant of the Monod equation.
Because of this nonlinearity, determining the equilibrium values of the
concentrations of the organisms in the food web is a superficially
complex problem. I show that the nonlinearity of the differential
equations can be overcome through a simple transformation that produces
a set of linear equations that can be readily solved with simple matrix
algebra for the equilibrium concentration values. I illustrate the
technique with a simple linear food chain and with the more complex food
web model of Laws et al. [Global Biogeochemical Cycles 14: 1231-1246
(2000)].
Kitack Lee1, S.D. Choi1, G.H. Park1, R. Wanninkhof2, J.L. Bullister3, R.A. Feely3, R.M. Key4, F.J. Millero5, T.-H. Peng2 and C.L. Sabine3,6
Anthropogenic CO2 in the Atlantic Ocean
1 SEE, Pohang University of Science and Technology, Pohang, Korea, email: ktl@postech.ac.kr
2 Atlantic Oceanographic and Meteorological Laboratory, NOAA, Miami
3 Pacific Marine Environmental Laboratory, NOAA, Seattle
4 AOSP, Princeton University, Princeton, New Jersey
5 RSMAS, University of Miami, Miami
6 JISAO, University of Washington, Seattle
ABSTRACT:
The anthropogenic CO2 concentration in the Atlantic is separated from
the large pool of dissolved inorganic carbon (CT) using a quasi-conservative
quantity DC* (Gruber et al., GBC, 1996):
Where CTEQ is the CT in equilibrium with a preindustrial atmospheric CO2 concentration of 280 uatm at in situ S, T, and preformed alkalinity value, ATo. The O2 and O2SAT are in situ and saturation concentration of oxygen, respectively, S is salinity, and T is temperature (oC). The values of DC* reflect not only the excess CO2 but also the air-sea disequilibrium (DCDISEQ) at the time the water lost contact with the atmosphere. The DCDISEQ term is better estimated in this study by using the Optimum Multiparameter (OMP) analysis, which allows for more accurate determination of mixing coefficients for various water types.
This improved method was applied to new carbon dataset collected as part
of World Hydrographic Program of the World Ocean Circulation Experiment
(WOCE) and the Ocean-Atmosphere Carbon Exchange Study (OACES) of the
National Oceanic and Atmospheric Administration (NOAA) between 1990 and
1998. In addition to the U.S. cruises, a significant number of European
cruises were included in the combined dataset, which finally has data
from 23 cruises. We will also present comparison of our results with
those obtained by Gruber (GBC, 1998) using the TTO/NAS, TTO/TAS, and
SAVE dataset.
Andrew W. Leising1, Wendy C. Gentleman1, Bruce W. Frost1, Jim Murray1 and Suzanne Strom2
Modeling the HNLC condition: some issues and constraints
1 University of Washington, School of Oceanography
2 Shannon Pt. Marine Lab, Western Washington University
ABSTRACT:
One of the main issues for constructing a mechanistic-based ecosystem model
is the determination of the proper transfer functions (e.g. a
microzooplankton's grazing functional response) between different
components or "boxes" of a model. Understanding how the choice of a
particular transfer function affects a model is especially critical in
oligotrophic regions or ecosystems where there are tight couplings between
the microzooplankton and their phytoplankton prey, since both the uptake
rates of the phytoplankton and the grazing rates of the microzooplankton
may be of similar order. High-Nitrate, Low-Chlorophyll (HNLC) regions fall
into this category, as phytoplankton production is co-limited by
iron-limitation and heavy microzooplankton grazing pressure. Changes in
the primary productivity of HNLC regions are of critical importance to
atmosphere-ocean carbon flux, as HNLC regions may release large amounts of
carbon to the atmosphere, rather than sequester it. Here, we show examples
of some of the critical issues concerning the uptake and transfer functions
within the phytoplankton-microzooplankton realm, which we believe are
important for constraining more complicated models. For both phytoplankton
and zooplankton, an important realization is that these organisms utilize
multiple (often 2 or more) nutrient sources, which adds additional
complexity to the mathematics used to describe their overall functional
responses. First, we show examples of the various functions used to
describe the uptake of multiple nutritional sources; these functions often
sacrifice biological reality for mathematical convenience. Second, weexamined the sensitivity of one of the most common single nutrient
responses for microzooplankton- the Mechalis-Menton relationship, with or
without a feeding threshold - in a simple NPZ model under steady and
variable physical forcing. Third, we examined a fairly complicated
multiple nutrient uptake scenario involving mixotrophic algae which eat
prey AND take up inorganics. Finally, we examined the historical data on
phytoplankton new vs total production (as proxies for the different
nutrient sources) in order to gain a better understanding of the possible
mechanisms controlling these factors, and thus providing better constraints
to future modeling efforts.
A three-dimensional, multi-nutrient, size-structured ecosystem model for the North Atlantic
1 School of Oceanography, Univ. Washington
P.O. Box 355351, Seattle, WA 98195
2 WHOI, Woods Hole, MA 02543-1541
ABSTRACT:
The magnitude of carbon fixation and export from the upper ocean by marine
biological processes is a key variable in quantifying the flux of carbon
between the ocean and the atmosphere, and our current inability to predict the
ocean response to and feedbacks on anthropogenic perturbations is one of the
major uncertainties for projecting future climate change. The synthesis phase
of the Joint Global Ocean Flux Study has demonstrated that the combination of
data from extensive field programs and remote sensing, and numerical coupled
physical-biogeochemical models is a powerful tool for understanding and
quantifying ocean biogeochemical processes and their potential future
responses to anthropogenic perturbations. In this study, we incorporate a
relatively complex ecosystem model into a three-dimensional, general ocean
circulation model for the North Atlantic. The ecosystem model accounts for
multi-element nutrient limitation and incorporates a more realistic,
mechanistic based phytoplankton growth and photoadaptation model. Model
results are compared with field data from time series stations, process
oriented studies sites, and SeaWiFS imagery.
Ivan Lima1, Luanne Thompson1, Steven Emerson1 and Paul Quay1
Investigation of the physical controls of the biological pump of carbon in the subtropical North Pacific
1 School of Oceanography, Univ. Washington
ABSTRACT:
The ocean plays a fundamental role in the global carbon cycle and climate
system as a major sink for anthropogenic carbon from fossil fuel burning and
land use change. Our current inability to predict the ocean response to and
feedbacks on anthropogenic perturbations is one of the major uncertainties for
projecting future climate change. The rate of mixed layer-thermocline exchange
is one of the primary factors controlling the oceanic uptake of anthropogenic
CO2 in the subtropical gyre. This is primarily through the solubility pump.
However, the processes controlling the biological pump of carbon is especially
uncertain in the large subtropical gyres. As a first step to investigate the
biological pump, in this study, CFCs are incorporated as tracers into a
layered isopycnal general circulation model of the North Pacific to evaluate
thermocline ventilation rates. The conservation properties of the isopycnal
model make it ideal for studying the physical control of tracer distributions.
The physical control of CFCs will lead to better understanding of other
tracers that effect the biology. The next step will be to investigate the
oxygen in the model, and ultimately the nutrient supply to the euphotic zone.
Preliminary results are presented and discussed focusing on the interannual
variability of the thermocline ventilation and its implications for biological
production and export of organic carbon.
E. Litchman1, C.A. Klausmeier2, B. van de Schootbrugge1, O. Schofield1 and P.G. Falkowski1
Applying Phytoplankton Community Models to Understanding Phytoplankton Distributions in the Paleoocean
1 Institute of Marine and Coastal Sciences, Rutgers University, New Brunswick, NJ
2 Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ
ABSTRACT:
Phytoplankton community structure has profound effects on major
biogeochemical cycles in the ocean. Understanding past and present shifts
in phytoplankton community composition is essential for predicting future
global change. One of the biggest community shifts in the past occurred
in the Mesozoic: from the ocean dominated by chlorophytes to the ocean
dominated by chromophytes (diatoms, coccolithophores, dinoflagellates).
What lead to the decline of green algae and rise to prominence of
chromophytes? Answering these questions may provide new insights
into the modern distribution and ecological niches of the key functional
groups. Here we develop a relatively simple phytoplankton community model
to explore potential mechanisms of community changes in the modern ocean
and the paleoocean. The model was verified with the JGOFS data from
several sites. The goal of the verification procedure was to obtain
qualitative agreement with the data, with an emphasis on presence or
absence of certain functional/taxonomic groups, seasonal succession,
nutrient concentrations and drawdown patterns. The model was then used to
examine the hypotheses for the occurrence of the contrasting
phytoplankton communities in the Mesozoic ocean: prasinophyte-dominated
vs. dinoflagellate-dominated communities of the lower Jurassic.
Surface Bomb D14C and Surface Residence Time in Ocean Biogeochemistry Models
1 AOS Program, Princeton Univ., Princeton, NJ 08544-0710 USA
2 PMEL/NOAA, Seattle, WA 98115 USA
ABSTRACT:
We compare simulations of anthropogenic CO2 and bomb radiocarbon
distribution from a suite of Princeton Ocean Biogeochemical Models and
models participating in Ocean Carbon Cycle Model Intercomparison Project.
We show that the uptake of anthropogenic CO2 is primarily determined by
vertical diffusion coefficient and secondarily by lateral eddy diffusion
coefficient. Models appear to overestimate the uptake of anthropogenic
tracers in the Southern Ocean, where convection is enhanced in order to
simulate more correctly the deep ocean ventilation. Because radiocarbon,
being a carbon isotope, has approximately a 10-year equilibration time
scale, its surface concentration is determined largely by surface
residence time. We formulate different methods of simulating the surface
ocean age and relate it to surface bomb D14C.
D.J. McGillicuddy, Jr.1, V.K. Kosnyrev1, E.N. Sweeney1 and K.O. Buesseler1
Modeling Mesoscale Biogeochemical Processes in a Topex/Poseidon Diamond Surrounding the U.S. JGOFS Bermuda Atlantic Time-series Study
1 Woods Hole Oceanographic Institution, Woods Hole, MA 02543
ABSTRACT:
An interdisciplinary modeling system has been configured in
the Topex/Poseidon (T/P) "diamond" surrounding the Bermuda Atlantic
Time-series (BATS) site. After extensive experimentation with
the treatment of the open boundary conditions,
a realistic hindcast of sea level variations in the interior
of the domain has been achieved by prescribing information only along the
boundaries.
The time series of RMS difference between simulated and observed
SLA fields for the entire altimetric record available to date
shows hindcast skill that is in most cases the same order as
the altimetric measurement error (3-5cm).
The T/P diamond model is being used to diagnose mesoscale
biogeochemical processes in a retrospective analysis of BATS data.
This activity was begun with an attempt to
interpret a three-year time series record of particle flux based on
thorium-234 measurements made by K.O. Buesseler. During this time period,
there were three anomalously high flux events. Analysis of
contemporaneous results from the T/P diamond model reveals that
each of the three events took place when eddy features were present.
The first two (June 1993 and August 1994) were
associated with cyclonic features (negative sea level anomalies),
while the last one (July 1995)
was associated with with a positive sea level anomaly.
Concurrent hydrographic measurements reveal the latter to be
associated with a so-called "Mode water eddy," a thick bolus
of 18-degree water which depresses the main thermocline and lifts
the seasonal thermocline. Previous work has shown that both
cyclones and Mode water eddies can inject nutrients into the
euphotic zone, causing the accumulation of phytoplankton biomass
in their interiors. Thus the high particulate flux events
inferred from the thoriu m-234 flux measurements are consistent
with these eddy-driven mechanisms.
Galen McKinley1, Mick Follows1 and John Marshall1
Interannual Variability of Air-Sea Fluxes of CO2 and O2
1 Department of Earth, Atmospheric, and Planetary Sciences, MIT 54-1517, Cambridge, MA 02139
ABSTRACT:
We use an ocean general circulation model to study the mechanisms of
air-sea O2 and CO2 flux variability, and consider the importance of this
variability to the estimation of global CO2 sinks (Keeling et al., Nature,
358, 1996; Bender et al., Global. Biogeochem. Cycles, 10, 1996; Manning,
PhD UCSD, 2001). Mean O2 and CO2 concentrations and air-sea fluxes are
estimated from a multi-decadal (1980-98) model integration of the global
offline MITgcm (Marshall et al., J. Geophys. Res., 120, 1997a,b; McKinley
et al., Geophys. Res. Let. 27. 2000). The mean air-sea CO2 flux is
consistent with the study of Takahashi et al. (Proc. CO2 in the Oceans,
1999) in all regions, and the mean O2 flux is consistent with the results
of Ganachaud (ScD MIT, 1999) in all regions except the Southern Ocean.
Interannual variability in air-sea CO2 and O2 fluxes has extremes of ±0.5 PgC/y and +70/-100 Tmol/y, respectively. Globally integrated variability in O2 and CO2 air-sea fluxes is dominantly forced by the El Niño / Southern Oscillation cycle. Interannual variability of the O2 flux in the North Atlantic is also significant on the global scale. The global impact of high latitude CO2 flux variability is small.
We find the interannual variability of air-sea O2 fluxes to be large
enough such that it should not be neglected in estimates of the
interannual variability in land and ocean CO2 sinks based on atmospheric
O2/N2 observations. In conclusion, we illustrate that estimates of CO2
sink variability from independent methods are converging toward an ocean
sink variability of <1 PgC/y and a land sink variability of approximately
2 PgC/y for the 1980's and 90's.
Ben I. McNeil1, Robert M. Key1, Andrew R. Jacobson1, Louis I. Gordon2 and Jorge L. Sarmiento1
Remineralization ratios in the subsurface Indian Ocean
1 AOS Program, Princeton Univ., NJ, USA
2 College of Oceanic and Atmospheric Science, Oregon State Univ., OR,
USA
ABSTRACT:
The subsurface (>500m) remineralization ratios for carbon and nutrients
were determined using Monte Carlo simulations of a weighted linear least
squares inversion for all available data taken during the Indian Ocean
WOCE program. For carbon, the anthropogenic CO2 signal was subtracted
from the data while the effects of denitrification and calcium carbonate
dissolution on all parameters were included in the technique. We find the
remineralization ratios (P/N/O/Corg) to increase considerably with depth
from 1/141/-14510/1078 in the upper ocean (500-1500m) to 1/140.5/-17515
/12510 in the deep ocean (>2000m). Although C/P and O/P increased
considerably with depth suggesting preferential remineralization of
phosphate in the upper water column, we did not find any significant
change in N/P. The increase in C/P and C/N with depth is consistent with
sediment trap results and points to possible biases in models that use
constant remineralization ratios for simulations of the biological carbon
pump.
Alexey V. Mishonov1, Wilford D. Gardner1 and Mary Jo Richardson1
Using the SeaWiFS data for POC assessment: which data product to use?
1 Department of Oceanography, Texas A&M University, College Station, TX, 77843
ABSTRACT:
Transmissometer data were collected during six South Atlantic Ventilation
Experiment (SAVE) hydrographic cruises conducted from November 1987 to March
1989 on the R/V Knorr and Melville.
A total of 361 beam attenuation profiles (see Fig. 1) were made with a
SeaTech transmissometer interfaced with a CTD/rosette. The regression
between beam attenuation and POC for the open Atlantic Ocean waters derived
from our previous research and enhanced by data from the Bermuda Atlantic
Time Series (BATS) was applied in order to obtain the particulate organic
carbon concentration.
These data were processed and examined as vertical sections of the surface
500m. Although the data were not synoptic, data were mapped in plan view for
presentation and analysis (Fig. 1).
Data were integrated over the upper 30m depth for comparison with the
distribution of optical data obtained from SeaWiFS.
No synchronous satellite data are available for those years, but our data
were compared with several satellite-derived variables from other years for
comparable seasons. The highest correlation was found between POC concentration and normalized
water leaving radiance at 555 nm. Other SeaWiFS-derived variables:
chlorophyll concentration, diffuse attenuation coefficient at 490 nm and
integral chlorophyll integrated over the upper optical depth were also
processed but show less satisfactory correlation.
Mathieu Mongin1,2 and David M. Nelson2
Simulation of upper-ocean biogeochemistry in the western Sargasso Sea with a flexible-composition phytoplankton model. I. Time courses of nutrients and phytoplankton biomass in the upper 200 m
1 Institut Universitaire Européen de la Mer, Technopôle Brest-Iroise, Place Nicolas Copernic, 29280 Plouzané (France).
2 College of Oceanic and Atmospheric Sciences, Oregon State University, Corvallis, Oregon 97311, U.S.A.
ABSTRACT:
We have developed a one-dimensional model of C, N and Si cycling in the
upper ocean, in which biogenic material is produced by two phytoplankton
groups: diatoms and nanophytoplankton. This model differs from other
such models mainly in that it permits the elemental composition of the
phytoplankton (C:N and Si:N ratios of diatoms and C:N ratios of
nanophytoplankton) to vary freely with time and depth in response to
light and nutrient availability. The growth rate of each phytoplankton
group is controlled by the most limiting resource (light, N or Si) in
accordance with the `cell quota' control mechanism first described
by Michael Droop almost 30 years ago. Growth of each group becomes
light-limited only when its C:N ratio is < 5.0 (mol/mol), N-limited
only when that ratio exceeds 10.0 and diatom growth becomes Si-limited
only when their Si:N ratio is < 0.6. The model thus allows phytoplankton
growth and uptake of non-limiting nutrients to continue - within limits -
even when light or concentrations of limiting nutrients severely limit
rates of photosynthesis or nutrient uptake. Under those conditions the
phytoplankton becomes deficient in C, N or Si, but continues to grow
until that deficiency becomes severe enough to limit growth. Besides
letting the phytoplankton respond to differential nutrient availability,
the model accounts for the known differences in the light dependence
of photosynthesis, nitrate uptake, ammonium uptake and silicic acid uptake.
We applied this model to the U.S. JGOFS Bermuda Atlantic Time-series Study (BATS) site for the years 1992 - 1995, a time period for which we have data on all processes considered by the model (including Si cycling and diatom productivity). Meteorological forcing was based on outputs of the European Centre Model for Weather Forecasting (ECMWF), and the physical and optical parts of the model were as developed earlier by Anderson and Pondaven (submitted). Very little `tuning' (manipulating of parameter values to obtain the best fit to the data record) was done. Instead, we chose parameter values consistent with data from phytoplankton culture studies or with field measurements at the BATS site.
The minimally tuned model reproduces the time courses of nitrate, silicic acid, chlorophyll, particulate organic carbon (POC) and biogenic silica in the upper 200 m reasonably well throughout the 1992 - 1995 time period. C:N ratios of both diatoms and nanophytoplankton are typically 9.0 - 10.0, and always significantly above the Redfield ratio of 6.6, in the upper 50 m each summer and autumn, reflecting strong N limitation. These ratios decrease to 5.0 - 6.0 the deep chlorophyll maximum (DCM) in summer and autumn, and throughout the upper water column during the spring bloom. These lower C:N ratios develop in response to greater N availability both during the bloom and in the DCM as well as lower irradiance in the DCM.
Nanophytoplankton is the dominant component of phytoplankton biomass
(both as POC and as chlorophyll) at all depths and at all times.
Diatom biomass reaches a maximum of ~30% of the total phytoplankton
biomass in the deeper portions of the DCM in summer.
Mathieu Mongin1,2 and David M. Nelson2
Simulation of upper-ocean biogeochemistry in the western Sargasso Sea with a flexible-composition phytoplankton model. II. Primary production, nutrient uptake and nutrient regeneration
1 Institut Universitaire Européen de la Mer, Technopôle Brest-Iroise, Place Nicolas Copernic, 29280 Plouzané (France).
2 College of Oceanic and Atmospheric Sciences, Oregon State University, Corvallis, Oregon 97311, U.S.A.
ABSTRACT:
The flexible-composition phytoplankton model described in Part I also
provides simulations of the major biogeochemical fluxes of C, N and Si
in the upper 200 m. Simulated primary productivity ranged interannually
from 117.9 to 149.6
g C m-2 y-1
(mean 131.6) during the 1992 - 1995 period, somewhat lower than the 116.0 - 188.5 6
g C m-2 y-1
range (mean 154.2) estimated from
14C productivity data. Annualized f-ratios,
calculated as vertically integrated annual nitrate uptake/annual
(nitrate + ammonium) uptake, show little interannual change at
0.26±0.03. These f-ratios represent a composite for the upper 200 m
over the year; f-ratios are lowest (0.1) in the upper 75 m in summer
and autumn, significantly higher (0.2 - 0.3) within the DCM and highest
(0.4 - 0.6) throughout the surface layer during the spring bloom of each
year.
The model appears to require significant rates of nitrification (bacterially mediated oxidation of ammonium to nitrate) in the upper 200 m. Without this nitrification, ammonium builds up to unrealistically high concentrations (0.8 - 1.0 µM) between 100 and 170 m and nitrate is completely depleted (to < 1 nM) in the surface layer throughout the summer. The integrated annual nitrification in the upper 200 m that we estimate from model simulations ranges interannually from 222 to 310 mmol N m-2 y-1, which represents 63 - 77% of the annual uptake of nitrate by phytoplankton in the euphotic zone. Using the model outputs we have calculated an f-ratio, which is calculated as:
Nitrate uptake - Nitrification
Nitrate uptake + ammonium uptake
when all rates are integrated for the year in the upper 200 m. This f-ratio ranges interannually only from 0.048 to 0.096, implying that ~90 - 95% of the N taken up annually by phytoplankton is remineralized either to ammonium or to nitrate in the upper 200 m. If these estimates are even close to correct, our simulations tend to support the conclusion of Lipschultz (2001) that nitrate is not a purely `new' nutrient in the upper 200 of in the western Sargasso Sea.
The simulations imply that production of biogenic silica by diatoms at
the BATS site ranges interannually from
162 to 247 mmol Si m-2 y-1
(mean 204), somewhat lower than the data-based estimate of
~240 mmol Si m-2 y-1
made by Nelson and Brzezinski (1997). These silica fluxes imply that
diatoms are responsible for ~25 - 30% of the annual primary production
at the BATS site. Perhaps surprisingly, the diatoms' contribution
to annual new production is considerably lower (14 - 19%) as a
consequence of their assumed higher KS
for nitrate uptake.
Modeling Southern Ocean Carbon Fluxes
1 University of California, Irvine, Dept. of Earth System Science, Irvine, CA. jkmoore@ucar.edu
ABSTRACT:
A decade ago the Southern Ocean was one of the most under-sampled,
under-studied regions of the world ocean. Since then there have been
numerous in situ studies in this region that have provided modelers with the
critical data needed to constrain/evaluate model output. This talk will
begin with a satellite overview of the Southern Ocean focusing on regional
variability and the role of Southern Ocean fronts. Model estimates of
atmospheric iron deposition to the Southern Ocean within mineral dust
for modern times and at the Last Glacial Maximum (LGM) will be presented.
Sensitivity to variations in dust deposition using a global mixed surface
layer ecosystem model (Moore et al., 2002) will be examined. Preliminary
results from a global 3D ecosystem model will be used to look at how
the factors limiting phytoplankton growth in the Southern Ocean vary over
seasonal timescales. Lastly, differences in dust deposition and sea ice
cover at the LGM will be discussed in terms of how these may have influenced
carbon cycling in the Southern Ocean.
J. Keith Moore1, Scott Doney2 and Keith Lindsay3
Phytoplankton Functional Groups and Oceanic Carbon Cycling
1 University of California, Irvine, Dept. of Earth System Science, Irvine, CA. jkmoore@ucar.edu
2 Woods Hole Oceanographic Institution, Woods Hole, MA. sdoney@whoi.edu
3 National Center for Atmospheric Research, Boulder, CO.
ABSTRACT:
A modified version of the Moore et al. (2002) marine ecosystem
model that includes several key functional groups of phytoplankton and
allows for multiple potentially limiting nutrients has been incorporated
into the ocean component of the NCAR Community Climate System Model.
The ecosystem model is coupled with a full biogeochemical module that
includes carbonate system dynamics and air-sea gas exchange of oxygen
and carbon dioxide. Phytoplankton functional groups represented include
diatoms, nitrogen-fixing diazotrophs, coccolithophores, and
picoplankton. Phytoplankton growth rates are a function of available
light, nitrogen, phosphorus, iron and (for the diatoms) silicon. The
inclusion of an explicit iron cycle, including the atmospheric source
from dust deposition, allows the model to capture the observed High
Nutrient, Low Chlorophyll conditions in the subarctic and equatorial
Pacific, and in the Southern Ocean. Model results are compared with
global in situ nutrient measurements and satellite-based estimates of
surface chlorophyll concentrations and primary production. Controls on
phytoplankton growth rates at the global scale are examined.
Ragu Murtugudde1 and Jim Christian1
Decadal variability in the tropical ecosystems
1 ESSIC, Univ of MD, College Park, MD 20742
ABSTRACT:
While the tropical Pacific is dominated by ENSO, the Atlantic has zonal
and meridional modes of variability on interannual time-scales. An
interdecadal regime shift has been noted in the Pacific and studied
widely for its signatures in the marin ecosystem from primary producers
to fisheries. It has been shown recently that a simultaneous regime
shift also occurs in the Atlantic and Indian Oceans in terms of a
thermocline/nitracline shift. The effects of this shift on the marine
ecosystems and the characteristics of this decadal variability are
studied in a coupled biological-physical model. Most of the variability
at these time-scales is associated with the large phytoplankton
suggesting consequences for the oceanic carbon cycle. The tropical
Atlantic appears to have undergone a change in its primary model of
interannual varaibility from a predominantly meridional to zonal or
Atlantic Niño model after 1976. The stronger and more frequent El Niños
in the Pacific are obviously manifest in the ecosystem response in terms
of reduced primary production in the east and enhanced entrainment in
the western Pacific warm pool. The details of the model simulations of
the circulation and ecosystem are presented.
Payal Parekh1*, Mick Follows1 and Ed Boyle1
Controls on deep water iron distribution
1 M.I.T., Department of Earth, Atmospheric, and Planetary Sciences, *MIT/WHOI Joint Program
ABSTRACT:
Waters upwelling to the surface ocean are deficient in iron relative
to other nutrients in terms of the requirements for biological
productivity. The extent of this deficit, and whether it may be
compensated locally by aeolian deposition, depends upon the balance
of ocean transport and biogeochemical mechanisms. We examine mechanisms
which may control the global, deep ocean iron distribution in the context
of a simplified ocean transport and biogeochemistry model.
The six box global ocean model includes coupled phosphorous and iron
cycles with prescribed atmospheric deposition of iron and ocean
circulation. Export production is parameterized simply, limited by
phosphate and iron availability in the surface ocean.
We compare several parameterizations of the deep water, geochemical processes affecting iron based on scavenging and backscavenging, analagous to the inferred properties of thorium, and complexation, the binding of iron to organic ligands. If complexation is not represented, provided that a ratio of scavenging to backscavenging rates of ~.01 is chosen the scavenging-backscavenging model can reproduce the observed, basin to basin, deep water gradients of iron. The introduction of a strong ligand into the model changes the balances, reducing the significance of backscavenging. The observed deep water gradients can still be reproduced. In addition, this model predicts that over 95% of the iron is organically bound and also leads to the presence of excess, uncomplexed ligand, in agreement with observations, but not captured in previous global models. Sensitivity tests indicate that deep water Fe gradients are sensitive to the scavenging rate and total ligand concentration. The observed iron distribution can be reproduced with a broad range of total ligand concentrations in combination with the appropriate scavenging rate.
These simplified models reinforce the concept that the deep water iron
distribution is controlled by a complex balance of ocean transports,
complexation, scavenging onto particles, and regionally varying aeolian
dust deposition. The idealized model provides a testbed for examining
basic parameterizations and in which to perform sensitivity studies.
The study also suggests a strategy for modeling the iron cycle, and its
effect on regional productivity, in global biogeochemical models.
Tsung-Hung Peng1 and Yuan-Hui Li2
Penetration of Anthropogenic CO2 in the Oceans Based on Analysis of Recent WOCE/JGOFS/OACES Carbon Data Using the Remineralization Ratios Obtained by the New Three-End-Member Mixing Model
1 NOAA/AOML, Ocean Chemistry Division, Miami, FL 33149
2 Department of Oceanography, University of Hawaii, Honolulu, HI 96822
ABSTRACT:
In a recent report (Li and Peng, 2002), a new three-end-member mixing
model is used to obtain remineralization ratios of organic matter in the
water column. Remineralization ratios
(P/N/Corg/-O2)
of organic matter in the deep water column change systematically from the
northern Atlantic to the Southern Oceans, then to the equatorial Indian and the
northern Pacific oceans, more or less along the global ocean circulation route
of deep water. Average remineralization ratios of organic matter for the
northern Atlantic Ocean are
P/N/Corg/-O2 =
1/(16±1)/(73±8)/(137±7),
and for the Southern Oceans
P/N/Corg/-O2 =
1/(15±1)/(80±3)/(133±5).
Those values are similar to the traditional Redfield ratios of
P/N/Corg/-O2 =
1/16/106/138
for marine plankton, except for the low
Corg/P ratio.
Average remineralization ratios for the equatorial Indian Ocean are
P/N/Corg/-O2 =
1/(10±1)/(94±5)/(130±7),
and for the northern Pacific Ocean
P/N/Corg/-O2 =
1/(13±1)/(124±11)/(162±11).
The apparent low N/P ratio for both ocean basins suggests that organic
nitrogen was converted partly into gaseous
N2O and
N2
by bacteria through nitrification/denitrification processes in a low-oxygen
or reducing micro-environment of organic matter throughout the oxygenated
water column. The actual N/P ratio of remineralized organic matter is probably
around 15±1. The
O2/Corg
ratio of remineralized organic matter also decreases systematically along the
global ocean circulation route of deep water, indicating changes in relative
proportions of biomoledules such as lipids, proteins, nucleic acids, and
carbohydrates.
In contrast, uniform remineralization ratios are assumed for almost all the current calculations using C* method for the anthropogenic CO2 inventory in the three major oceans (for example, Gruber et al., 1996; Gruber, 1998; Sabine et al., 1999 and 2002; and Feely et al., 2001). The question that needs to be asked is: how much difference in anthropogenic CO2 penetration into the ocean could be made if the new results of variable ratios are used as compared with those of traditional methods where the uniform remineralization ratios have been used. In this study, a new method derived from our mixing model, which is different from C* method, is developed for estimating the penetration of anthropogenic CO2 into the ocean, specifically using the current variable remineralization ratios. This new method will be described in details, and comparison of current results based on HOT station north of Hawaii will be made between using uniform remineralization ratios and variable remineralization ratios.
References:
Feely, R. A., C. L. Sabine, T. Takahashi, and R. Wanninkhof, Uptake and storage of carbon dioxide in the ocean, Oceanography 14,18-32, 2001.
Gruber, N., j. L. Sarmiento, and T. F. Stocker, An improved method for detecting anthropogenic CO2 in the oceans, Global Biogeochem. Cycles 10, 809-837, 1996.
Gruber, Anthropogenic CO2 in the Atlantic Ocean, Global Biogeochemical Cycles, 12, 165-191, 1998.
Li, Y.-H. and T.-H. Peng, Latitudinal change of remineralization ratios in the oceans and its implication for nutrient cycles. Global Biogeochem. Cycles, (submitted) 2002.
Sabine, C.L., R.M. Key, K.M. Johnson, F.J. Millero, A. Poisson, J.L. Sarmiento, D.W.R. Wallace, and C.D. Winn, Anthropogenic CO2 inventory of the Indian Ocean, Global Biogeochem. Cycles, 13, 179-198, 1999.
Sabine, C. L., R. A. Feely, R. M. Key, J. L. Bullister, F. J. Millero, K. Lee, T.-H. Peng, B. Tilbrook, T. Ono, and C. S. Wang, Distribution of anthropogenic CO2 in the Pacific Ocean, Global Biogeochem. Cycles, (in press) 2002.
B. B. Prézelin1, E. E. Hofmann2 and J. M. Klinck2
Physical Forcing of Phytoplankton Community Structure in Continental Shelf Waters of the western Antarctic Peninsula
1 Mar. Sci. Inst. and Dept Ecology, Evolution and Marine Biology,
Univ, California, Santa Barbara, CA 93106
2 Center for Coastal Phys. Oceanogr., Old Dominion Univ. Norfolk, Virginia 23529
ABSTRACT:
A previous study of the Western Antarctic Peninsula (WAP) continental
shelf that was based upon a multidisciplinary data set collected during
austral summer of January 1993 identified a mechanism previously unrecognized
that sets up a physical and chemical structure that supports enhanced
biological production (Prézelin et al. 2000). This biological production
occurs when the southern boundary of the Antarctic Circumpolar Current
(ACC) flows along the shelf edge, which produces upwelling and intrusions
of nutrient-rich Upper Circumpolar Deep Water (UCDW) onto the shelf,
thereby allowing site-specific diatom-dominated phytoplankton communities
to develop. The enhanced biological production potentially affects
all components of the marine food web in this region. In this analysis,
we extend the area and seasons studied through similar analyses of
multidisciplinary data sets collected on four additional cruises
that cover all seasons. We find that this newly recognized forcing
is active in other regions of the WAP shelf where similar conditions
are found, is episodic, and is forced by non-seasonal physical processes.
The meander frequency of the ACC has consequences for the timing
and location of UCDW intrusions. When multiple intrusions are observed,
each event may be in a different stage. Further, the occurrence of
an event in one area does not necessarily imply that similar events
are ongoing in other areas along the shelf.
While these UCDW upwelling events originate along the outer shelf,
they have a signature that extends into the inner shelf region because
of the deep topography with allows the inner shelf to be connected
to the outer shelf. The frontal boundary between the intruded water
and the shelf water is variable in location because of the episodic
nature of the onshelf intrusions, being moved further inshore when
one of these events is occurring. The frontal boundaries are characterized
by distinct phytoplankton communities whose distribution along the
circulation structure is identifiable by the unique presence of a
chemotaxonomic marker (Chlorophyll b) in the near surface waters.
These observations show clearly that the phytoplankton community
structure on the WAP shelf is determined by physical forcing. Moreover,
variability in this physical forcing, such as ma